The ESF meeting on the proteomics, epigenetics and pharmacogenetics of pendrin

Cellular Physiology and Biochemistry

Volumn 28, Issue 3, 2011, Pages 377-384

  Dossena, Silvia ^a   Nofziger, Charity ^a   Lang, Florian ^b   Valenti, Giovanna ^c   Paulmichl, Markus ^a  

^a PARACELSUS MEDICAL UNIVERSITY   (Austria)

^b UNIVERSITY OF TÜBINGEN   (Germany)

^c UNIVERSITY OF BARI   (Italy)

Author keywords

EVA; Functional test; Inherited hearing loss; Ion transport; Pendred syndrome; Pendrin; SLC26A4

Indexed keywords

PENDRIN;

CHRONIC OBSTRUCTIVE LUNG DISEASE; DISEASE EXACERBATION; EPIGENETICS; HEARING LOSS; HUMAN; HYPERTENSION; PATHOGENESIS; PENDRED SYNDROME; PHARMACOGENETICS; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN FUNCTION; PROTEIN LOCALIZATION; PROTEOMICS; RESPIRATORY DISTRESS; REVIEW; UPREGULATION;

EID: 82255163792     PISSN: 10158987     EISSN: 14219778     Source Type: Journal    
DOI: 10.1159/000335101     Document Type: Review

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